meddevicedb.com FDA Device Reference

Black Diamond

K222323 Class II Traditional
Decision Date
2023-06-23
Sponsor / Applicant
Elevate Oral Care, LLC

Technical Specification

510(k) Submission ID K222323
Product Code PHR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3260
Decision Date 2023-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Black Diamond received FDA 510(k) clearance under submission number K222323, sponsored by Elevate Oral Care, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2023-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code PHR and 21 CFR 872.3260, within the Dental review panel as a Class II device.